Found: 21
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Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.
- Published in:
- 2010
- By:
- Publication type:
- Report
The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males.
- Published in:
- Human Genetics, 2006, v. 120, n. 4, p. 447, doi. 10.1007/s00439-006-0198-x
- By:
- Publication type:
- Article
No Equity, No Triple Aim: Strategic Proposals to Advance Health Equity in a Volatile Policy Environment.
- Published in:
- American Journal of Public Health, 2017, v. 107, p. S223, doi. 10.2105/AJPH.2017.304000
- By:
- Publication type:
- Article
Telomeres and Telomerase in Human Health and Disease.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2002, v. 15, n. 3, p. 229, doi. 10.1515/jpem.2002.15.3.229
- By:
- Publication type:
- Article
Induced pluripotent stem cells as a model for telomeric abnormalities in ICF type I syndrome.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 14, p. 3629, doi. 10.1093/hmg/ddu071
- By:
- Publication type:
- Article
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 9, p. 1816, doi. 10.1093/hmg/ddq040
- By:
- Publication type:
- Article
Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 18, p. 2776, doi. 10.1093/hmg/ddn177
- By:
- Publication type:
- Article
Telomeres in ICF syndrome cells are vulnerable to DNA damage due to elevated DNA:RNA hybrids.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 14015, doi. 10.1038/ncomms14015
- By:
- Publication type:
- Article
Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction.
- Published in:
- eLife, 2019, p. 1, doi. 10.7554/eLife.47859
- By:
- Publication type:
- Article
MBTPS1 regulates proliferation of colorectal cancer primarily through its action on sterol regulatory elementbinding proteins.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.1004014
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- Publication type:
- Article
Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation.
- Published in:
- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0014342
- By:
- Publication type:
- Article
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.
- Published in:
- Biomolecules (2218-273X), 2023, v. 13, n. 12, p. 1717, doi. 10.3390/biom13121717
- By:
- Publication type:
- Article
Biology of advanced uveal melanoma and next steps for clinical therapeutics.
- Published in:
- Pigment Cell & Melanoma Research, 2015, v. 28, n. 2, p. 135, doi. 10.1111/pcmr.12304
- By:
- Publication type:
- Article
Pima County COVID-19 vaccine solutions dashboard project: lessons learned.
- Published in:
- Frontiers in Digital Health, 2024, p. 1, doi. 10.3389/fdgth.2024.1345451
- By:
- Publication type:
- Article
Epigenetic Characteristics of Human Subtelomeres Vary in Cells Utilizing the Alternative Lengthening of Telomeres (ALT) Pathway.
- Published in:
- Life (2075-1729), 2021, v. 11, n. 4, p. 278, doi. 10.3390/life11040278
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- Publication type:
- Article
Regulation of telomeric function by DNA methylation differs between humans and mice.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 19, p. 3197, doi. 10.1093/hmg/ddaa206
- By:
- Publication type:
- Article
Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 20, p. 3568, doi. 10.1093/hmg/ddy265
- By:
- Publication type:
- Article
Non-random length distribution of individual telomeres in immunodeficiency, centromeric instability and facial anomalies syndrome, type I.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 21, p. 4244, doi. 10.1093/hmg/ddx313
- By:
- Publication type:
- Article
Quantitative digital in situ senescence-associated Β-galactosidase assay.
- Published in:
- BMC Cell Biology, 2011, v. 12, n. 1, p. 16, doi. 10.1186/1471-2121-12-16
- By:
- Publication type:
- Article
Dp140: a novel 140 kDa CNS transcript from the dystrophin locus.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 3, p. 329
- By:
- Publication type:
- Article
DNA:RNA hybrids at telomeres – when it is better to be out of the (R) loop.
- Published in:
- FEBS Journal, 2018, v. 285, n. 14, p. 2552, doi. 10.1111/febs.14464
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- Publication type:
- Article